Circumventing complement C3 interference in the analysis of carbohydrate-deficient transferrin in fresh serum

被引:12
作者
Beisler, AT
Kelly, RH
Landers, JP
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22901 USA
[2] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
[3] Presbyterian Univ Hosp, Dept Pathol, Pittsburgh, PA 15213 USA
[4] Univ Virginia, Hlth Sci Ctr, Dept Pathol, Charlottesville, VA 22908 USA
关键词
capillary electrophoresis; beta-globulins; transferrin; CDT; complement;
D O I
10.1006/abio.2000.4717
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method for preventing interference by the glycoprotein complement C3 and its beta-globulin split products in the capillary electrophoretic analysis of carbohydrate-deficient transferrin was developed. Inulin was used to activate the alternate complement pathway and convert native C3 into various degradation products whose electrophoretic mobility no longer coincides with the transferrin glycoforms. Capillary electrophoresis and zone electrophoresis on agarose gel were used to monitor reaction conditions for alternate complement pathway activation. Incubation of 50 mu L of fresh serum with 180 mu L of a 50 mg/mL inulin slurry for 12 h removed the native C3 peak from the beta region. Inulin treatment did not affect electrophoretic behavior of other beta-globulins, including transferrin, Altering the electrophoretic behavior of complement C3, by treating fresh serum with inulin, permits rapid capillary electrophoresis evaluation of carbohydrate-deficient transferrin glycoforms. (C) 2000 Academic Press.
引用
收藏
页码:143 / 150
页数:8
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